Sarah E. Heron

<i>KCNQ2</i> encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

Sarah Weckhuysen, Simone Mandelstam, Arvid Suls et al. · Annals of Neurology · 2011 · 494 citations

Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism

Michael Gill, G Daly, Sarah E. Heron et al. · Molecular Psychiatry · 1997 · 489 citations

Adhd, Neuropsychological Functioning, Brain Function +9

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy

Sarah E. Heron, Katherine R. Smith, Melanie Bahlo et al. · Nature Genetics · 2012 · 405 citations · Full text

Channelopathies, Missense Mutations, Hyperpolarization (Biology) +11

Sodium-channel defects in benign familial neonatal-infantile seizures

Sarah E. Heron, Kathryn M. Crossland, Eva Andermann et al. · The Lancet · 2002 · 375 citations

Developmental Anomaly, Sodium-channel Defects, Neurophysiology +5

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Leanne M. Dibbens, Boukje de Vries, Simona Donatello et al. · Nature Genetics · 2013 · 358 citations

Mendelian Disorder, Genetic Disorder, Genetics +8